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Assessment of the incidence of surgical site infections after digestive surgery with preoperative oral antibiotics.

Not Applicable
Conditions
Patients with lower digestive surgery (Inflammatory bowel disease, Colorectal cancer)
Registration Number
JPRN-UMIN000015460
Lead Sponsor
Dep. Surgery, Tohoku University Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
200
Inclusion Criteria

Not provided

Exclusion Criteria

Patients with allergy for Ciprofloxacin or Metronidazole.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The rate of surgical site infection at 30th days after surgery
Secondary Outcome Measures
NameTimeMethod
Safety of the preoperative oral antibiotics.
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